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No relevant pharmacokinetic drug–drug interaction between nintedanib and pirfenidone

No relevant pharmacokinetic drug–drug interaction between nintedanib and pirfenidone
No relevant pharmacokinetic drug–drug interaction between nintedanib and pirfenidone
Nintedanib and pirfenidone are approved treatments for idiopathic pulmonary fibrosis (IPF). This open-label, two-group trial investigated the pharmacokinetic drug–drug interaction between these two drugs in patients with IPF.

Subjects not treated with antifibrotics at screening (group 1, n=20) received a single nintedanib dose (150 mg) followed by pirfenidone (titrated to 801 mg thrice daily) for 3 weeks, with a further single nintedanib dose (150 mg) on the last day (day 23). Subjects treated with pirfenidone at screening (group 2, n=17) continued to receive pirfenidone alone (801 mg thrice daily) for 7 days, then co-administered with nintedanib (150 mg twice daily) for a further 7 days, before single doses of both treatments on day 16.

In group 1, adjusted geometric mean (gMean) ratios (with/without pirfenidone) were 88.6% and 80.6% for nintedanib area under the plasma concentration–time curve (AUC) and maximum plasma concentration (Cmax), respectively. In group 2, gMean ratios (with/without nintedanib) were 97.2% and 99.5% for pirfenidone AUC and Cmax, respectively. For all parameters, the 90% confidence intervals included 100%, suggesting similar exposure for administration alone and when co-administered. Both treatments were well tolerated.

These data indicate there is no relevant pharmacokinetic drug–drug interaction between nintedanib and pirfenidone when co-administered in IPF patients.
0903-1936
Richeldi, Luca
47177d9c-731a-49a1-9cc6-4ac8f6bbbf26
Fletcher, Sophie
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Adamali, Huzaifa
488339d5-0b2b-47b7-adec-bf3c6b039be3
Chaudhuri, Nazia
21496f8d-8b7b-4275-ac86-7a494871c9e1
Wiebe, Sabrina
b98fac7d-ac4b-497a-b4c3-e8de165e684d
Wind, Sven
869279da-07b8-4f6c-a886-66a2617276ff
Hohl, Kathrin
78e351f3-d277-489e-b9cb-74e34e38f757
Baker, Andrew
1cc4e39e-3550-4cf1-8482-174ccf231c27
Schlenker-Herceg, Rozsa
b99d9236-8d93-43d8-8111-fa21b1f31e0b
Stowasser, Susanne
db03e3f9-5df8-403d-b6f7-5284a506fd94
Maher, Toby M.
6c166764-7a4e-4d20-b528-381a7218ea0b
Richeldi, Luca
47177d9c-731a-49a1-9cc6-4ac8f6bbbf26
Fletcher, Sophie
71599088-9df7-4d4a-8570-aef773ead0fe
Adamali, Huzaifa
488339d5-0b2b-47b7-adec-bf3c6b039be3
Chaudhuri, Nazia
21496f8d-8b7b-4275-ac86-7a494871c9e1
Wiebe, Sabrina
b98fac7d-ac4b-497a-b4c3-e8de165e684d
Wind, Sven
869279da-07b8-4f6c-a886-66a2617276ff
Hohl, Kathrin
78e351f3-d277-489e-b9cb-74e34e38f757
Baker, Andrew
1cc4e39e-3550-4cf1-8482-174ccf231c27
Schlenker-Herceg, Rozsa
b99d9236-8d93-43d8-8111-fa21b1f31e0b
Stowasser, Susanne
db03e3f9-5df8-403d-b6f7-5284a506fd94
Maher, Toby M.
6c166764-7a4e-4d20-b528-381a7218ea0b

Richeldi, Luca, Fletcher, Sophie, Adamali, Huzaifa, Chaudhuri, Nazia, Wiebe, Sabrina, Wind, Sven, Hohl, Kathrin, Baker, Andrew, Schlenker-Herceg, Rozsa, Stowasser, Susanne and Maher, Toby M. (2019) No relevant pharmacokinetic drug–drug interaction between nintedanib and pirfenidone. European Respiratory Journal. (doi:10.1183/13993003.01060-2018).

Record type: Article

Abstract

Nintedanib and pirfenidone are approved treatments for idiopathic pulmonary fibrosis (IPF). This open-label, two-group trial investigated the pharmacokinetic drug–drug interaction between these two drugs in patients with IPF.

Subjects not treated with antifibrotics at screening (group 1, n=20) received a single nintedanib dose (150 mg) followed by pirfenidone (titrated to 801 mg thrice daily) for 3 weeks, with a further single nintedanib dose (150 mg) on the last day (day 23). Subjects treated with pirfenidone at screening (group 2, n=17) continued to receive pirfenidone alone (801 mg thrice daily) for 7 days, then co-administered with nintedanib (150 mg twice daily) for a further 7 days, before single doses of both treatments on day 16.

In group 1, adjusted geometric mean (gMean) ratios (with/without pirfenidone) were 88.6% and 80.6% for nintedanib area under the plasma concentration–time curve (AUC) and maximum plasma concentration (Cmax), respectively. In group 2, gMean ratios (with/without nintedanib) were 97.2% and 99.5% for pirfenidone AUC and Cmax, respectively. For all parameters, the 90% confidence intervals included 100%, suggesting similar exposure for administration alone and when co-administered. Both treatments were well tolerated.

These data indicate there is no relevant pharmacokinetic drug–drug interaction between nintedanib and pirfenidone when co-administered in IPF patients.

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Accepted/In Press date: 28 October 2018
e-pub ahead of print date: 10 January 2019

Identifiers

Local EPrints ID: 478807
URI: http://eprints.soton.ac.uk/id/eprint/478807
ISSN: 0903-1936
PURE UUID: 63c419cb-e14d-4dd7-90ad-b0207440409f
ORCID for Sophie Fletcher: ORCID iD orcid.org/0000-0002-5633-905X

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Date deposited: 10 Jul 2023 16:58
Last modified: 21 Sep 2024 02:15

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Contributors

Author: Luca Richeldi
Author: Sophie Fletcher ORCID iD
Author: Huzaifa Adamali
Author: Nazia Chaudhuri
Author: Sabrina Wiebe
Author: Sven Wind
Author: Kathrin Hohl
Author: Andrew Baker
Author: Rozsa Schlenker-Herceg
Author: Susanne Stowasser
Author: Toby M. Maher

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